A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037480



Internal ID19126699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:53343054..53529811hg38UCSC Ensembl
Innerchr10:55102814..55289571hg19UCSC Ensembl
Innerchr10:54772820..54959577hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38186758
hg19186758
hg18186758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505038
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037480
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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